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Endocrine, Metabolic & Immune Disorders - Drug Targets

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ISSN (Print): 1871-5303
ISSN (Online): 2212-3873

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General Review Article

Agammaglobulinemia: Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management

Author(s): Salar Pashangzadeh, Reza Yazdani*, Farzad Nazari, Gholamreza Azizi, Hassan Abolhassani and Asghar Aghamohammadi*

Volume 20, Issue 9, 2020

Page: [1434 - 1447] Pages: 14

DOI: 10.2174/1871530320666200508114349

Price: $65

Abstract

Agammaglobulinemia is a type of primary antibody deficiencies, characterized by severe reduction in serum level of all types of immunoglobulins level and absence of B cells in the peripheral blood. X-linked and various autosomal recessive/dominant mutations have been identified underlying the pathogenesis of this disorder. Affected patients present a broad range of clinical manifestations, including respiratory infections, gastrointestinal complications, Enterovirus infections, autoimmunity, and malignancies. This disease can be controlled by different therapeutic strategies. In this review, we describe different aspects of agammaglobulinemia such as epidemiology, pathogenesis, clinical phenotype, diagnosis, management, and prognosis of congenital agammaglobulinemia.

Keywords: Primary immunodeficiency, agammaglobulinemia, epidemiology, pathogenesis, clinical phenotype, diagnosis, management, prognosis.

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Graphical Abstract

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